Sarah Daly

Sarah Daly

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Sarah Daly

Sarah Daly

Publications by authors named "Sarah Daly"

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Improved spectrophotometric assay for lytic polysaccharide monooxygenase.

Biotechnol Biofuels 2019 5;12:283. Epub 2019 Dec 5.

1Biocatalysis and Biosensor Laboratory, Department of Food Science and Technology, BOKU-University of Natural Resources and Life Sciences, Muthgasse 18, 1190 Vienna, Austria.

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http://dx.doi.org/10.1186/s13068-019-1624-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6894463PMC
December 2019

Redundancy in Anaerobic Digestion Microbiomes during Disturbances by the Antibiotic Monensin.

Appl Environ Microbiol 2018 05 16;84(9). Epub 2018 Apr 16.

Department of Biological and Environmental Engineering, Cornell University, Ithaca, New York, USA

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http://dx.doi.org/10.1128/AEM.02692-17DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5930344PMC
May 2018

HelpDesk: How accurate are point-of-care urine drug screens in patients taking chronic opioid therapy?

J Fam Pract 2018 03;67(3):177

Utah Valley Family Medicine Residency, Provo, UT, USA.

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March 2018

Predictors of Acute Myocardial Infarction.

Am Fam Physician 2017 Sep;96(5):328

Utah Valley Family Medicine Residency, Provo, UT, USA.

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September 2017

Phenotypic Heterogeneity in a Congenital Disorder of Glycosylation Caused by Mutations in STT3A.

J Child Neurol 2017 05 16;32(6):560-565. Epub 2017 Mar 16.

3 Manchester Centre for Genomic Medicine, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.

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http://dx.doi.org/10.1177/0883073817696816DOI Listing
May 2017

Clinical Inquiries: Does vitamin D without calcium reduce fracture risk?

J Fam Pract 2016 12;65(12):933-934

University of Iowa, Iowa City, IA, USA.

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December 2016

Leri's pleonosteosis, a congenital rheumatic disease, results from microduplication at 8q22.1 encompassing GDF6 and SDC2 and provides insight into systemic sclerosis pathogenesis.

Ann Rheum Dis 2015 Jun 17;74(6):1249-56. Epub 2014 Jan 17.

Faculty of Medical and Human Sciences, Manchester Centre for Genomic Medicine, Institute of Human Development, University of Manchester, Manchester Academic Health Science Centre (MAHSC), Manchester, UK Manchester Centre for Genomic Medicine, Central Manchester University Hospitals NHS Foundation Trust, MAHSC, Manchester, UK.

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http://dx.doi.org/10.1136/annrheumdis-2013-204309DOI Listing
June 2015

Is nonoperative therapy as effective as surgery for meniscal injuries?

J Fam Pract 2015 May;64(5):311-2

Utah Valley Family Medicine Residency, Provo, UT, USA.

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May 2015

Mutations in LZTR1 add to the complex heterogeneity of schwannomatosis.

Neurology 2015 Jan 5;84(2):141-7. Epub 2014 Dec 5.

From the Manchester Centre for Genomic Medicine (M.J.S., W.G.N., D.G.E.) and University of Manchester Biomedical Imaging Institute (S.J.M.), Manchester Academic Health Sciences Centre, and Centre for Imaging Sciences (S.J.M.), University of Manchester, UK; Service de Dermatologie (S.B.) and Service de Genetique Medicale (B.I.), CHU Nantes, France; Institut für Klinische Chemie und Laboratoriumsdiagnostik Universitätsklinikum Jena (C.B.), Germany; Centre for Genomic Medicine (S.G.W., S.S.B., J.O., B.A., S.B.D., J.E.U., W.G.N., D.G.E.), St. Mary's Hospital, Central Manchester University Hospitals NHS Foundation Trust, UK; INSERM U830 (W.R., F.B.), Laboratoire de Genetique et Biologie des Cancers, Paris, France; Department of Clinical Genetics (A.F.), Alder Hey Children's Hospital, Liverpool, UK; Department of Medical Genetics (C.F.R.), Oslo University Hospital, Norway; International Neuroscience Institute (A.S.), Hannover, Germany; Department of Cellular Pathology and Greater Manchester Neurosciences Centre (D.d.P.), Salford Royal Hospitals NHS Foundation Trust; Department of Clinical Genetics (D.H.), Oxford Radcliffe Hospitals NHS Trust, UK; and Institut Curie (F.B.), SIRIC and Departement d'Oncologie Pediatrique d'Adolescents et Jeunes Adultes, Paris, France.

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http://www.neurology.org/content/84/2/141.full.pdf
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http://www.neurology.org/cgi/doi/10.1212/WNL.000000000000112
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http://dx.doi.org/10.1212/WNL.0000000000001129DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4336087PMC
January 2015

Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations.

J Clin Oncol 2014 Dec 17;32(36):4155-61. Epub 2014 Nov 17.

Miriam J. Smith, Simon G. Williams, Sanjeev S. Bhaskar, James O'Sullivan, Beverley Anderson, Sarah B. Daly, Jill E. Urquhart, Zaynab Bholah, William G. Newman, and D. Gareth R. Evans, Manchester Centre for Genomic Medicine, University of Manchester, Manchester Academic Health Sciences Centre, and Central Manchester University Hospitals National Health Service (NHS) Foundation Trust; Deemesh Oudit, Christie NHS Foundation Trust; Edmund Cheesman and Anna Kelsey, Central Manchester University Hospital NHS Foundation Trust, Royal Manchester Children's Hospital; Martin G. McCabe, Institute of Cancer Sciences, University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom; and Christian Beetz, Institut für Klinische Chemie und Laboratoriumsdiagnostik Universitätsklinikum Jena, Jena, Germany.

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http://jco.ascopubs.org/content/early/2014/11/20/JCO.2014.58
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http://jco.ascopubs.org/cgi/doi/10.1200/JCO.2014.58.2569
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http://dx.doi.org/10.1200/JCO.2014.58.2569DOI Listing
December 2014

Chronic cough and OSA: an underappreciated relationship.

Lung 2014 Feb;192(1):21-5

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http://dx.doi.org/10.1007/s00408-013-9534-9DOI Listing
February 2014

Chronic cough and OSA: a new association?

J Clin Sleep Med 2011 Dec;7(6):669-77

Department of Medicine, Utah Valley Pulmonary Clinic, Provo, UT 84604, USA.

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http://dx.doi.org/10.5664/jcsm.1482DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3227716PMC
December 2011

Chronic cough and obstructive sleep apnea in a community-based pulmonary practice.

Cough 2010 Apr 15;6(1). Epub 2010 Apr 15.

Intermountain Utah Valley Pulmonary Clinic, 1055N, 300W, Provo, UT 84604, USA.

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http://dx.doi.org/10.1186/1745-9974-6-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861010PMC
April 2010

Identification of MPL W515L/K mutations in patients with primary myelofibrosis and essential thrombocythaemia by allele-specific polymerase chain reaction.

Acta Haematol 2009 10;121(4):221-2. Epub 2009 Jun 10.

Cancer Molecular Diagnostics, St. James's Hospital, Dublin 8, Ireland.

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http://dx.doi.org/10.1159/000224333DOI Listing
August 2009

EQUAL-quant: an international external quality assessment scheme for real-time PCR.

Clin Chem 2006 Aug 1;52(8):1584-91. Epub 2006 Jun 1.

National Genetics Reference Laboratory (Manchester), St. Mary's Hospital, Manchester, UK, and Institute of Medical Statistics and Biometry, University of Milan, Italy.

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http://www.clinchem.org/content/52/8/1584.full.pdf
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http://www.clinchem.org/cgi/doi/10.1373/clinchem.2005.066019
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http://dx.doi.org/10.1373/clinchem.2005.066019DOI Listing
August 2006